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Study of Karenitecin (BNP1350) to treat Malignant Melanoma



Study of Karenitecin (BNP1350) to treat Malignant Melanoma

For Condition: Melanoma,Neoplasm
Status: No longer recruiting
Sponsor(s): BioNumerik Pharmaceuticals, Inc. ,
Synopsis: The purpose of this study is to determine if Karenitecin (BNP1350) is effective in the treatment of Malignant Melanoma.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: - Confirmed diagnosis of malignant melanoma - Measurable disease - Granulocytes 1,500/µl, Platelets 100,000/µl, Creatinine ULN, Bilirubin 1.5 mg/dl, AST 2.5 x ULN - No prior treatment with other camptothecin drug. - 21 days since completion of prior chemotherapy, 6 weeks since prior Mitomycin-C - ECOG Performance Status 0-1 - Negative pregnancy test for female patients
Total Enrollment: 

Location and Contact Information:

For Information call 210-614-1701 for a site near you
Tampa,  Florida, 
United States
 


Additional Information:
Study ID Numbers:
  KTN23106; 
Study Start Date: 
Record last reviewed: August 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00062491

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